Characterisation of Two Oxidosqualene Cyclases Responsible for Triterpenoid Biosynthesis in Ilex asprella

被引:33
作者
Zheng, Xiasheng [1 ,2 ]
Luo, Xiuxiu [1 ]
Ye, Guobing [1 ]
Chen, Ye [1 ]
Ji, Xiaoyu [1 ]
Wen, Lingling [1 ]
Xu, Yaping [1 ]
Xu, Hui [1 ]
Zhan, Ruoting [1 ]
Chen, Weiwen [1 ]
机构
[1] Guangzhou Univ Chinese Med, Key Lab Chinese Med Resource Lingnan, Res Ctr Chinese Herbal Resource Sci & Engn, Guangzhou 510006, Guangdong, Peoples R China
[2] Zhongshan Zhongzhi Pharmaceut Grp, Key Lab Technol Breaking Cell Wall & Applicat Chi, Zhongshan 528437, Peoples R China
关键词
BETA-AMYRIN SYNTHASE; LUPEOL SYNTHASE; SAPONINS; GENE; EXPRESSION; DIVERSITY; SQUALENE; CLONING; CDNA; ACID;
D O I
10.3390/ijms16023564
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ilex asprella, a plant widely used as a folk herbal drug in southern China, produces and stores a large amount of triterpenoid saponins, most of which are of the alpha-amyrin type. In this study, two oxidosqualene cyclase (OSC) cDNAs, IaAS1 and IaAS2, were cloned from the I. asprella root. Functional characterisation was performed by heterologous expression in the yeast Saccharomyces cerevisiae. Analysis of the resulting products by gas chromatography (GC) and gas chromatography-mass spectrometry (GC-MS) showed that both genes encode a mixed amyrin synthase, producing alpha-amyrin and beta-amyrin at different ratios. IaAS1, which mainly produces alpha-amyrin, is the second triterpene synthase so far identified in which the level of alpha-amyrin produced is >= 80% of total amyrin production. By contrast, IaAS2 mainly synthesises beta-amyrin, with a yield of 95%. Gene expression patterns of these two amyrin synthases in roots and leaves of I. asprella were found to be consistent with the content patterns of total saponins. Finally, phylogenetic analysis and multiple sequence alignment of the two amyrin synthases against several known OSCs from other plants were conducted to further elucidate their evolutionary relationship.
引用
收藏
页码:3564 / 3578
页数:15
相关论文
共 28 条
[1]   MOLECULAR-CLONING, CHARACTERIZATION, AND FUNCTIONAL EXPRESSION OF RAT OXIDOSQUALENE CYCLASE CDNA [J].
ABE, I ;
PRESTWICH, GD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (20) :9274-9278
[2]   Enzymatic synthesis of cyclic triterpenes [J].
Abe, Ikuro .
NATURAL PRODUCT REPORTS, 2007, 24 (06) :1311-1331
[3]   Herbivore-induced responses in alfalfa (Medicago sativa) [J].
Agrell, J ;
Oleszek, W ;
Stochmal, A ;
Olsen, M ;
Anderson, P .
JOURNAL OF CHEMICAL ECOLOGY, 2003, 29 (02) :303-320
[4]   An unusual plant triterpene synthase with predominant α-amyrin-producing activity identified by characterizing oxidosqualene cyclases from Malus x domestica [J].
Brendolise, Cyril ;
Yauk, Yar-Khing ;
Eberhard, Ellen D. ;
Wang, Mindy ;
Chagne, David ;
Andre, Christelle ;
Greenwood, David R. ;
Beuning, Lesley L. .
FEBS JOURNAL, 2011, 278 (14) :2485-2499
[5]  
Gietz RD, 2002, METHOD ENZYMOL, V350, P87
[6]  
Haralampidis K, 2002, ADV BIOCHEM ENG BIOT, V75, P31
[7]   Differential expression of three oxidosqualene cyclase mRNAs in Glycyrrhiza glabra [J].
Hayashi, H ;
Huang, P ;
Takada, S ;
Obinata, M ;
Inoue, K ;
Shibuya, M ;
Ebizuka, Y .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2004, 27 (07) :1086-1092
[8]   Molecular characterization of the pentacyclic triterpenoid biosynthetic pathway in Catharanthus roseus [J].
Huang, Lili ;
Li, Jia ;
Ye, Hechun ;
Li, Changfu ;
Wang, Hong ;
Liu, Benye ;
Zhang, Yansheng .
PLANTA, 2012, 236 (05) :1571-1581
[9]   Ursolic acid is a PPAR-α agonist that regulates hepatic lipid metabolism [J].
Jia, Yaoyao ;
Bhuiyan, Muhammad Javidul Haque ;
Jun, Hee-jin ;
Lee, Ji Hae ;
Hoang, Minh Hien ;
Lee, Hak-Ju ;
Kim, Nahyun ;
Lee, Dongho ;
Hwang, Kwang Yeon ;
Hwang, Bang Yeon ;
Choi, Dal-Woong ;
Lee, Sung-Joon .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2011, 21 (19) :5876-5880
[10]   Functional Characterization and Localization of Pneumocystis carinii Lanosterol Synthase [J].
Joffrion, Tiffany M. ;
Collins, Margaret S. ;
Sesterhenn, Thomas ;
Cushion, Melanie T. .
EUKARYOTIC CELL, 2010, 9 (01) :107-115